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Eine Ebene höherGruppiert nach: Dokumententyp |
Veröffentlichungsdatum
Anzahl der Publikationen: 9
2010
Blaschek, Astrid; Lohse, P.; Huss, K.; Borggraefe, I.; Mueller-Felber, W.; Heinen, F.; Hohlfeld, R. und Kümpfel, T.
(2010):
Concurrent TNFRSF1A R92Q and pyrin E230K mutations in a child with multiple sclerosis.
In: Multiple Sclerosis, Bd. 16, Nr. 12: S. 1517-1520
[PDF, 179kB]
Schroepf, S.; Kappler, R.; Brand, S.; Prell, C.; Lohse, P.; Glas, J.; Hoster, Eva; Helmbrecht, J.; Ballauff, A.; Berger, M.; Schweinitz, D. von; Koletzko, Sibylle und Lacher, M.
(2010):
Strong overexpression of CXCR3 axis components in childhood inflammatory bowel disease.
In: Inflammatory Bowel Diseases, Bd. 16, Nr. 11: S. 1882-1890
Jürgens, Matthias; Brand, S.; Laubender, Rüdiger P.; Seiderer, Julia; Glas, Jürgen; Wetzke, M.; Wagner, J.; Pfennig, S.; Tillack, C.; Beigel, Florian; Weidinger, M.; Schnitzler, Fabian; Kreis, M. E.; Göke, Burkhard; Lohse, P.; Herrmann, K. und Ochsenkühn, Thomas
(2010):
The presence of fistulas and NOD2 homozygosity strongly predict intestinal stenosis in Crohn’s disease independent of the IL23R genotype.
In: Journal of Gastroenterology, Bd. 45, Nr. 7: S. 721-731
2006
Thalmaier, D.; Dambacher, J.; Seiderer, Julia; Konrad, A.; Schachinger, V.; Pfennig, S.; Otte, J. M.; Crispin, Alexander; Göke, Burkhard; Ochsenkühn, Thomas; Lohse, P. und Brand, S.
(2006):
The +1059G/C polymorphism in the C-reactive protein (CRP) gene is associated with involvement of the terminal ileum and decreased serum CRP levels in patients with Crohn’s disease.
In: Alimentary Pharmacology & Therapeutics, Bd. 24, Nr. 7: S. 1105-1115
Seiderer, Julia; Brand, S.; Herrmann, Karin A.; Schnitzler, Fabian; Hatz, R.; Crispin, Alexander; Pfennig, S.; Schoenberg, S. O.; Göke, Burkhard; Lohse, P. und Ochsenkühn, Thomas
(2006):
Predictive Value of the CARD15 Variant 1007fs for the Diagnosis of Intestinal Stenoses and the Need for Surgery in Crohn’s Disease in Clinical Practice: Results of a Prospective Study.
In: Inflammatory Bowel Diseases, Bd. 12, Nr. 12: S. 1114-1121
2005
Brand, S.; Staudinger, T.; Schnitzler, Fabian; Pfennig, S.; Hofbauer, K.; Dambacher, J.; Seiderer, Julia; Tillack, C.; Konrad, A.; Crispin, Alexander; Göke, Burkhard; Lohse, P. und Ochsenkühn, Thomas
(2005):
The role of Toll-like receptor 4 Asp299Gly and Thr399Ile polymorphisms and CARD15/NOD2 mutations in the susceptibility and phenotype of Crohn’s disease.
In: Inflammatory Bowel Diseases, Bd. 11, Nr. 7: S. 645-652
2004
Schiemann, Uwe; Müller-Koch, Y.; Gross, M.; Daum, J.; Lohse, P.; Baretton, G.; Muders, M.; Mussack, T.; Kopp, R. und Holinski-Feder, E.
(2004):
Extended microsatellite analysis in microsatellite stable, MSH2 and MLH1 mutation-negative HNPCC patients: Genetic reclassification and correlation with clinical features.
In: Digestion, Nr. 3: S. 166-176
[PDF, 221kB]
2003
Török, H. P.; Glas, J.; Lohse, P. und Folwaczny, Christian
(2003):
Alterations of the CARD15/NOD2 gene and the impact on management and treatment of Crohn's disease patients.
In: Digestive Diseases, Nr. 4: S. 339-345
[PDF, 106kB]
2001
Tautermann, G.; Ruebsamen, H.; Beck, M.; Dertinger, S.; Drexel, H. und Lohse, P.
(2001):
R116C mutation of cationic trypsinogen in a Turkish family with recurrent pancreatitis illustrates genetic microheterogeneity of hereditary pancreatitis.
In: Digestion, Nr. 4: S. 226-232
[PDF, 309kB]